US3896252A - Process of metal plating on plastics - Google Patents

Process of metal plating on plastics Download PDF

Info

Publication number
US3896252A
US3896252A US43945374A US3896252A US 3896252 A US3896252 A US 3896252A US 43945374 A US43945374 A US 43945374A US 3896252 A US3896252 A US 3896252A
Authority
US
United States
Prior art keywords
rubber
percent
polymer
anhydride
alcohol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
Inventor
Carole K Tuttle
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dow Chemical Co filed Critical Dow Chemical Co
Priority to US43945374 priority Critical patent/US3896252A/en
Application granted granted Critical
Publication of US3896252A publication Critical patent/US3896252A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/18Pretreatment of the material to be coated
    • C23C18/20Pretreatment of the material to be coated of organic surfaces, e.g. resins
    • C23C18/28Sensitising or activating
    • C23C18/30Activating or accelerating or sensitising with palladium or other noble metal
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/18Pretreatment of the material to be coated
    • C23C18/20Pretreatment of the material to be coated of organic surfaces, e.g. resins
    • C23C18/2006Pretreatment of the material to be coated of organic surfaces, e.g. resins by other methods than those of C23C18/22 - C23C18/30
    • C23C18/2046Pretreatment of the material to be coated of organic surfaces, e.g. resins by other methods than those of C23C18/22 - C23C18/30 by chemical pretreatment
    • C23C18/2073Multistep pretreatment
    • C23C18/2086Multistep pretreatment with use of organic or inorganic compounds other than metals, first
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/10Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern
    • H05K3/18Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material
    • H05K3/181Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/38Improvement of the adhesion between the insulating substrate and the metal
    • H05K3/381Improvement of the adhesion between the insulating substrate and the metal by special treatment of the substrate

Definitions

  • thermoplastic polymer employed in this invention is a rubber modified unsaturated carboxylic acid or anhydride containing polymer which is prepared by polymerizing the monomers inthe presence of the rubber in a finely divided form.
  • the surface to be metallized is first aminated with a solution of ethylenediamine or 1,3-diaminopropane in an inert solvent of about 50 to 100 volume percent of a water miscible organic solvent and O to about 50 percent water, then treated with a noble metal salt solution and thereafter with a reducing agent to produce a metallized surface having a resistance of 100 ohms/sq. or less.
  • the metallized surface can then be further plated by conventional means.
  • the process of this invention provides improvement in adhesion between the plastic and the metallic layer deposited thereon, simplification in processing, elimination of chromic acid oxidizing baths, and improvements in thermal resistance and other physical properties of the plated article.
  • the invention depends on using certain thermoplastic polymers.
  • the thermoplastic must contain a rubber modifier component in amounts of about 12 to 40 weight percent. It must also contain about 12 to 30 weight percent of an unsaturated acid or anhydride thereof and the balance to make 100 percent of one or more monomers copolymerized therewith.
  • the thermoplastic is the product of polymerizing the monomers in the presence of the rubber in a finely divided form.
  • the process comprises the step of aminating the surface to be metallized with a solution of ethylenediamine or l,3-diaminopropane in an inert solvent which is not a solvent for the thermoplastic polymer.
  • the solvent comprises about 50 to 100 volume percent of a water miscible organic solvent and O to about 50 volume percent of water.
  • the aminated surface is then treated with a noble metal salt solution such as silver and thereafter with a reducing agent to produce a metallized surface having a resistance of about 100 ohms/sq. or less.
  • ABS acrylonitrile/- butadiene/styrene
  • plastics of this invention provide higher heat distortion and other improvements in physical properties.
  • Essential to the invention is the use of a rubber modified thermoplastic polymer prepared by polymerizing an unsaturated carboxylic acid or anhydride with one or more copolymerizable monomers in the presence of the rubber in finely divided form.
  • the benefits of this invention are not obtained if the rubber is omitted or if the rubber is merely blended or milled with a polymer prepared from the above monomers.
  • Adhesion is somehow related to the presence of the rubber component although no adequate explanation is presently known for this feature of the invention. In any event, tests demonstrate that the rubber is necessary. For best results, the rubber should be as finely divided as possible since adhesion decreases with coarse rubber particles.
  • finely divided rubber it is meant rubber particles having an average particle diameter in the range of about 0.1 to 1p. with a maximum particle size of about 51L. Average particle diameters of 5-30p. and higher are considered coarse and unsuitable.
  • any of a variety of rubbers may be used such as natural rubber; rubbery copolymers of ethylene and propylene; conjugated diene rubbers such as polyisobutylene, polyisoprene and polybutadiene; copolymers of conjugate dienes and alkenyl aromatic monomers such as butadiene-styrene copolymers; nitrile rubbers such as a copolymer of butadiene and acrylonitrile; and the like.
  • Preferred rubbers are the butadiene-styrene copolymers especially the block copolymers. It is known to employ small amounts of other monomers such as acrylonitrile in preparing preferred rubbers.
  • Unsaturated carboxylic monomers include acrylic acid, methacrylic acid, ethacrylic acid, 3-butenoic acid, 4-pentenoic acid and the like as well as di and polycarboxylic acid monomers such as maleic acid, itaconic acid, fumaric acid, citraconic acid aconitic acid and the like.
  • the anhydrides of said diand polycarboxylic acids are preferred in this invention. Especially preferred is maleic anhydride.
  • Copolymerizable monomers may be selected from a wide variety of known monomers including the alkyl acrylates and methacrylates, alkenyl aromatics, vinyl ether and ester monomers, etc. Typical of such monomers are methyl ethyl and butyl acrylate and methacrylate; styrene, vinyl toluene, t-butyl styrene; vinyl methyl ether, vinyl acetate, etc. Preferred are the alkenyl aromatic monomers and styrene is especially preferred.
  • the rubber modified unsaturated carboxylic acid or anhydride containing thermoplastic polymer comprises from about 12 to 40 weight percent rubber, preferably about 16 to 22 percent; about 12 to 30 weight percent of said acid or anhydride, preferably about 12 to 25 weight percent; and the balance to make percent of one or more copolymerizable monomers. More preferably the acid or anhydride monomer comprises about 14 to 20 percent of the thermoplastic polymer. A certain minimum acid or anhydride content is necessary to obtain uniform metallization whereas at contents above the maximum solubilization of the polymer is a problem.
  • the process of this invention comprises the step of first aminating the surface to be metallized by contacting it with a solution of ethylenediamine or 1,3- diaminopropane in an inert solvent which is not a solvent for the thermoplastic polymer.
  • a solution of ethylenediamine or 1,3- diaminopropane in an inert solvent which is not a solvent for the thermoplastic polymer Following amination, the surface is treated with a noble metal salt solution. Examples of noble metal salts that may be used are silver nitrate, platinic chloride, auric chloride, palladium chloride, as well as complex metal salts such as diamminesilver (l) nitrate. Finally, the surface is contacted with a reducing agent to produce a metallized surface having a resistance of 100 ohms/sq. or less, preferably 50 ohms/sq. or less.
  • Typical reducing agents include formaldehyde, hydrazine, hydroxylamine, sodium borohydride, tartrates, hydroquinone and the like. Amination of the surface forms salts of the acid groups and halfamide and/or halfamide salts of the anhydride group.
  • the surface to be metallized is usually rinsed after each of the process steps and that each step require only a few minutes.
  • the time of contact can be extended but usually the necessary effect from each step occurs very rapidly and long contact times are neither necessary or desirable.
  • the inert solvent employed in the amination step comprises about 50 to 100 volume percent of a water miscible organic solvent and from to about 50 percent of water.
  • inert it is meant that the solvent has no adverse reactive effect on the diamines dissolved therein or on the thermoplastic polymer, i.e., it is not a solvent for the polymer or has no adverse effect with its functional groups under the conditions employed.
  • organic solvents are available including such solvents as dioxane, acetonitrile, dimethyl formamide and alcohols.
  • the alcohols are preferred as are the equal volume mixtures of alcohols with water.
  • the more preferred alcohols are methyl, ethyl and isopropyl alcohol.
  • Some of the above named organic solvents, such as the alcohols, may be used as the sole solvent whereas others are useful only as mixtures with water.
  • Aqueous solutions of the diamines utilized herein are not effective in producing the metal adhesion required and are therefor to be contrasted to agents such as aqueous hydrazine and hydroxylamine which recently have been found to be quite effective. Conversely, hydrazine and hydroxylamine are not effective as solutions in the solvent of this invention. No satisfactory explanation is yet available to explain these unexpected results but experimental evidence confirms them. This invention is even more unique in view of the generally poor results obtained with other amines as has been mentioned above and as will be shown later.
  • a rubber modified styrene-maleic anhydride thermoplastic was prepared by polymerizing styrene and maleic anhydride in the presence of a finely divided styrene-butadiene (30:70) block copolymer rubber (average particle size in the range of 0.5 to 11 with a maximum particle size of about 211.).
  • the polymer contained about 19% rubber, 16% maleic anhydride and the balance styrene.
  • the polymerization was effected in a ketone solvent at -135C using lauroyl peroxide as a catalyst.
  • An injection molded part of the above polymer was immersed in a 3M solution of ethylenediamine in a 1:1 (by volume) mixture of water and methyl alcohol for 10 minutes. Thereafter it was rinsed and then placed in a 0.3N Ag(NH NO bath for 5 minutes. After rinsing, the part was immersed in a reducing agent solution of 5% hydrazine in water.
  • the metallized surface produced had a resistance of 19 ohms/sq. and had excellent metallization.
  • EXAMPLE 3 The time sequence of example 2 was changed in the following test to 5 minutes of immersion in the ethylenediamine solution, 5 minutes immersion in 0.3N Ag N0 in 10% ammonia solution and 1 minute reduction in 5% hydrazine solution.
  • the part has a resistivity of 10 ohms/sq. and an average peel strength of 3.1 lbs/in. with a maximum of 3.5 lbs/in.
  • a process for metallizing plastic articles formed from a rubber modified unsaturated carboxylic acid or anhydride containing thermoplastic polymer which comprises the steps of a. aminating the surface to be metallized by contacting it with a solution of ethylenediamine or 1,3- diaminopropane in an inert solvent comprising from about 50 to 100 volume percent of a water miscible organic solvent and from 0 to about 50 percent water,
  • said rubber modified polymer contains about 12 to 40 weight percent rubber, about 12 to 30 weight percent of said acid or anhydride and the balance to make 100 percent of one or more monomers copolymerized therewith and wherein said polymer is the product of polymerizing the monomers in the presence of the rubber in a finely divided form.
  • a process for metallizing plastic articles formed from a rubber modified unsaturated dicarboxylic acid anhydride containing thermoplastic polymer which comprises the steps of a. aminating the surface to be metallized by contacting it with a solution of ethylenediamine or 1,3- diaminopropane in an inert solvent comprising from about 50 to 100 volume percent of a water miscible organic solvent and from O to about 50 percent water,
  • said rubber modified polymer contains about 12 to 40 weight percent rubber, about 12 to 30 weight percent of said anhydride and the balance to make 100 percent of one or more monomers copolymerizable therewith and wherein said polymer is the product of polymerizing the monomers in the presence of the rubber in a finely divided form.
  • polymer is a rubber modified polymer of said anhydride and an alkenyl aromatic monomer.

Abstract

The thermoplastic polymer employed in this invention is a rubber modified unsaturated carboxylic acid or anhydride containing polymer which is prepared by polymerizing the monomers in the presence of the rubber in a finely divided form. The surface to be metallized is first aminated with a solution of ethylenediamine or 1,3-diaminopropane in an inert solvent of about 50 to 100 volume percent of a water miscible organic solvent and 0 to about 50 percent water, then treated with a noble metal salt solution and thereafter with a reducing agent to produce a metallized surface having a resistance of 100 ohms/sq. or less. The metallized surface can then be further plated by conventional means.

Description

[ July 22, 1975 Tuttle PROCESS OF METAL PLATING 0N PLASTICS [75] Inventor: Carole K. Tuttle, Midland, Mich.
[73] Assignee: The Dow Chemical Company,
Midland, Mich.
[22] Filed: Feb. 4, 1974 [21] Appl. No.: 439,453
[52] 11.8. C1 427/306; 427/400 [51] Int. Cl C23c 3/02; B44d l/092 [58] Field of Search 260/880 B; 117/47 A, 118
[56] References Cited UNITED STATES PATENTS 3,222,218 12/1965 Beltzer et al ll7/47 A X 3,359,345 12/1967 Doak et al 260/880 B- 3,567,488 3/1971 Rathsack .1 117/47 A 3,649,713 3/1972 Chin et a1. 260/876 R 3,702,285 11/1972 Knorre et a1 117/47 A X Primary Examiner-Ralph S. Kendall Assistant Examiner-John D. Smith Attorney, Agent, or Firm-H. L. Aamoth [5 7] ABSTRACT The thermoplastic polymer employed in this invention is a rubber modified unsaturated carboxylic acid or anhydride containing polymer which is prepared by polymerizing the monomers inthe presence of the rubber in a finely divided form. The surface to be metallized is first aminated with a solution of ethylenediamine or 1,3-diaminopropane in an inert solvent of about 50 to 100 volume percent of a water miscible organic solvent and O to about 50 percent water, then treated with a noble metal salt solution and thereafter with a reducing agent to produce a metallized surface having a resistance of 100 ohms/sq. or less. The metallized surface can then be further plated by conventional means.
21 Claims, No Drawings PROCESS OF METAL PLATING ON PLASTICS BACKGROUND OF THE INVENTION Conventional plating of plastics, as pointed out in U.S. Pat. No. 3,556,955, conditions the plastic in a strong oxidizing solution, e.g. aqueous sulfuric acidchromic acid. The plastic is next sensitized in a solution of a reducing agent such as stannous chloride and then activated by immersion in a noble metal salt solution before passing the plastic to an electroless plating bath.
This general method with the prior art polymers suffers from numerous disadvantages among which are the complexities of the process and the hazards and dis posal problems with the chromic acid bath as well as lesser physical properties of the plated polymers. Various methods of overcoming some of these problems are proposed in U.S. Pat. Nos. 3,556,955 and 3,701,675. Polymers with acid groups or treated to have acid groups are neutralized with ammonia, alkali solutions or ethylenimine according to U.S. Pat. Nos. 3,567,488; 3,567,489 and 3,607,350. The polymers are then treated with a noble metal salt solution before being plated. U.S. Pat. No. 3,222,218 is similar to Czech Pat. No. 100,373 in that ion exchange groups on a polymer are treated with a noble metal salt and after ion exchange are reduced and then plated. Because plastic materials are non-conductive and inert to metals, adhesion of the metal plate to the plastic is a basic problem in the metallization of plastics.
SUMMARY OF THE INVENTION The process of this invention provides improvement in adhesion between the plastic and the metallic layer deposited thereon, simplification in processing, elimination of chromic acid oxidizing baths, and improvements in thermal resistance and other physical properties of the plated article.
First, the invention depends on using certain thermoplastic polymers. In particular, the thermoplastic must contain a rubber modifier component in amounts of about 12 to 40 weight percent. It must also contain about 12 to 30 weight percent of an unsaturated acid or anhydride thereof and the balance to make 100 percent of one or more monomers copolymerized therewith. The thermoplastic is the product of polymerizing the monomers in the presence of the rubber in a finely divided form.
Secondly, the process comprises the step of aminating the surface to be metallized with a solution of ethylenediamine or l,3-diaminopropane in an inert solvent which is not a solvent for the thermoplastic polymer. The solvent comprises about 50 to 100 volume percent of a water miscible organic solvent and O to about 50 volume percent of water. The aminated surface is then treated with a noble metal salt solution such as silver and thereafter with a reducing agent to produce a metallized surface having a resistance of about 100 ohms/sq. or less.
DESCRIPTION OF THE INVENTION Notwithstanding the art in the field of metallization of plastics, the most commonly accepted plastic material for this use is a polymer of acrylonitrile/- butadiene/styrene (commonly called ABS) and the process employed utilizes a chromic acid oxidizing bath and the subsequent steps previously noted. In fact, not all ABS polymers are generally suitable. Consequently,
there is a limited choice of suitable plastic materials from a commercial standpoint.
By this invention, another group of plastic materials may now be utilized and may be metallized by a different, simpler process than the old chromic acid process. In addition to providing good adhesion. the plastics of this invention provide higher heat distortion and other improvements in physical properties.
The results of this invention are considered unique and unexpected since similar results are not obtained if the rubber component is omitted and if other aminating agents are used in place of ethylenediamine or l,3- diaminopropane.
Essential to the invention is the use of a rubber modified thermoplastic polymer prepared by polymerizing an unsaturated carboxylic acid or anhydride with one or more copolymerizable monomers in the presence of the rubber in finely divided form. The benefits of this invention are not obtained if the rubber is omitted or if the rubber is merely blended or milled with a polymer prepared from the above monomers.
Adhesion is somehow related to the presence of the rubber component although no adequate explanation is presently known for this feature of the invention. In any event, tests demonstrate that the rubber is necessary. For best results, the rubber should be as finely divided as possible since adhesion decreases with coarse rubber particles. By finely divided rubber it is meant rubber particles having an average particle diameter in the range of about 0.1 to 1p. with a maximum particle size of about 51L. Average particle diameters of 5-30p. and higher are considered coarse and unsuitable.
While the presence of the rubber is important, any of a variety of rubbers (elastomers) may be used such as natural rubber; rubbery copolymers of ethylene and propylene; conjugated diene rubbers such as polyisobutylene, polyisoprene and polybutadiene; copolymers of conjugate dienes and alkenyl aromatic monomers such as butadiene-styrene copolymers; nitrile rubbers such as a copolymer of butadiene and acrylonitrile; and the like. Preferred rubbers are the butadiene-styrene copolymers especially the block copolymers. It is known to employ small amounts of other monomers such as acrylonitrile in preparing preferred rubbers.
Unsaturated carboxylic monomers include acrylic acid, methacrylic acid, ethacrylic acid, 3-butenoic acid, 4-pentenoic acid and the like as well as di and polycarboxylic acid monomers such as maleic acid, itaconic acid, fumaric acid, citraconic acid aconitic acid and the like. The anhydrides of said diand polycarboxylic acids are preferred in this invention. Especially preferred is maleic anhydride.
Copolymerizable monomers may be selected from a wide variety of known monomers including the alkyl acrylates and methacrylates, alkenyl aromatics, vinyl ether and ester monomers, etc. Typical of such monomers are methyl ethyl and butyl acrylate and methacrylate; styrene, vinyl toluene, t-butyl styrene; vinyl methyl ether, vinyl acetate, etc. Preferred are the alkenyl aromatic monomers and styrene is especially preferred.
The rubber modified unsaturated carboxylic acid or anhydride containing thermoplastic polymer comprises from about 12 to 40 weight percent rubber, preferably about 16 to 22 percent; about 12 to 30 weight percent of said acid or anhydride, preferably about 12 to 25 weight percent; and the balance to make percent of one or more copolymerizable monomers. More preferably the acid or anhydride monomer comprises about 14 to 20 percent of the thermoplastic polymer. A certain minimum acid or anhydride content is necessary to obtain uniform metallization whereas at contents above the maximum solubilization of the polymer is a problem.
The process of this invention comprises the step of first aminating the surface to be metallized by contacting it with a solution of ethylenediamine or 1,3- diaminopropane in an inert solvent which is not a solvent for the thermoplastic polymer. Following amination, the surface is treated with a noble metal salt solution. Examples of noble metal salts that may be used are silver nitrate, platinic chloride, auric chloride, palladium chloride, as well as complex metal salts such as diamminesilver (l) nitrate. Finally, the surface is contacted with a reducing agent to produce a metallized surface having a resistance of 100 ohms/sq. or less, preferably 50 ohms/sq. or less. Resistance of this magnitude is needed in order to deposit subsequent metal layers by conventional plating processes. Typical reducing agents include formaldehyde, hydrazine, hydroxylamine, sodium borohydride, tartrates, hydroquinone and the like. Amination of the surface forms salts of the acid groups and halfamide and/or halfamide salts of the anhydride group.
It is to be understood that the surface to be metallized is usually rinsed after each of the process steps and that each step require only a few minutes. The time of contact can be extended but usually the necessary effect from each step occurs very rapidly and long contact times are neither necessary or desirable.
The inert solvent employed in the amination step comprises about 50 to 100 volume percent of a water miscible organic solvent and from to about 50 percent of water. By inert it is meant that the solvent has no adverse reactive effect on the diamines dissolved therein or on the thermoplastic polymer, i.e., it is not a solvent for the polymer or has no adverse effect with its functional groups under the conditions employed.
A variety of useful organic solvents are available including such solvents as dioxane, acetonitrile, dimethyl formamide and alcohols. The alcohols are preferred as are the equal volume mixtures of alcohols with water. The more preferred alcohols are methyl, ethyl and isopropyl alcohol. Some of the above named organic solvents, such as the alcohols, may be used as the sole solvent whereas others are useful only as mixtures with water.
Aqueous solutions of the diamines utilized herein are not effective in producing the metal adhesion required and are therefor to be contrasted to agents such as aqueous hydrazine and hydroxylamine which recently have been found to be quite effective. Conversely, hydrazine and hydroxylamine are not effective as solutions in the solvent of this invention. No satisfactory explanation is yet available to explain these unexpected results but experimental evidence confirms them. This invention is even more unique in view of the generally poor results obtained with other amines as has been mentioned above and as will be shown later.
The following nonlimiting examples will further illustrate the invention.
EXAMPLE 1 A rubber modified styrene-maleic anhydride thermoplastic was prepared by polymerizing styrene and maleic anhydride in the presence of a finely divided styrene-butadiene (30:70) block copolymer rubber (average particle size in the range of 0.5 to 11 with a maximum particle size of about 211.). The polymer contained about 19% rubber, 16% maleic anhydride and the balance styrene. The polymerization was effected in a ketone solvent at -135C using lauroyl peroxide as a catalyst.
An injection molded part of the above polymer was immersed in a 3M solution of ethylenediamine in a 1:1 (by volume) mixture of water and methyl alcohol for 10 minutes. Thereafter it was rinsed and then placed in a 0.3N Ag(NH NO bath for 5 minutes. After rinsing, the part was immersed in a reducing agent solution of 5% hydrazine in water. The metallized surface produced had a resistance of 19 ohms/sq. and had excellent metallization.
Following the above procedure replacing ethylenediamine with 1,2-diaminopropane a metallized surface having resistance of 14-32 ohms/sq. was obtained. The part was well metallized as above.
EXAMPLE 2 Following the procedure of example 1, the following tests were made with ethylenediamine with the results below.
Surface* Peel Strength Resistivity, lbs/in.
ohms/sq. Ave. Max.
Average of tests 2.7 3.0
*Resistunce of metallized part before electroplating.
(from a copper pyrophosphate bath at 30-35 amps per sq. ft.). The peel strength was measured on an Instron Tester after the part had dried and aged for 24 hours or more. A 1 inch wide strip of metal plate was peeled off the sample at a angle to the surface at a rate of 1 inch/min.
EXAMPLE 3 The time sequence of example 2 was changed in the following test to 5 minutes of immersion in the ethylenediamine solution, 5 minutes immersion in 0.3N Ag N0 in 10% ammonia solution and 1 minute reduction in 5% hydrazine solution. A
Amine Reagent Peel Strength lbs/in.
Surface Resistivity.
ohms/sq. Ave. Max.
19 l 3 l7 l4 1 2 14 Average of tests The above tests were repeated with the polymer containing about 28% rubber.
These latter tests were repeated changing the initial immersion time from to minutes. The part has a resistivity of 10 ohms/sq. and an average peel strength of 3.1 lbs/in. with a maximum of 3.5 lbs/in.
EXAMPLE 4 In contrast to the above results, a number of other amines were tested in a similar manner and the results reported below. While metallization to some degree occurred in some cases, it was insufficient for subsequent plating purposes.
Surface Resistivity (ohms/sq.
Results no metallization v. sl. metallization no metallization 10 dull black, silver surface N.N-dimethyl hydrazine methyl hydrazine hydroxyethyl hydrazine methyl hydrazine* no metallization 10 v. 51. metallization no metallization no metallization 82-210; light metallization triethylene tetraamine diethylenetriamine pyridine morpholine hydroxyethylamine *noble metal was 0.3N AgNQ, in 10% ammonia EXAMPLE 5 The above tests were repeated using an aqueous solution of ethylenediamine but the results were erratic. While a silver metal deposit was obtained in one case having a resistance of 43-150 ohms/sq., subsequent electroplating resulted in bare spots and inhomogeneous plating.
EXAMPLE 6 The proportions of water to methanol were evaluated in another series of tests using 3M ethylenediamine and the above procedure with the results recorded below.
Volume Ratio Surface Resistivity CH OH/Water ohms/sq.
20/80 10 10 40/60 40. 13, 10 50/50 13, 9 60/40 9, l3, 8, 15 /20 9, l8, 9. l3 /0 8, l8, 9, 14
Except for the first test, the parts were electroplated. All parts plated well except for those prepared with the 40/60 solvent ratio. It can be seen therefore that consistent results are obtained with an alcohol to water ratio of 50/50 and higher and with methyl alcohol as the sole solvent.
EXAMPLE 7 Organic solvents other than methyl alcohol were tested by the above procedure using 3M ethylenediamine dissolved in a 1:1 v/v solvent of water and the organic solvent. The parts were tested for adhesion as before. The results are recorded below.
*1:1 v/v mixture with water An attempt was made to use tetrahydrofuran as the organic solvent but it dissolved the polymer. Based on the previous results, it can be seen that best results are obtained with the alcohols.
What is claimed is:
1. A process for metallizing plastic articles formed from a rubber modified unsaturated carboxylic acid or anhydride containing thermoplastic polymer which comprises the steps of a. aminating the surface to be metallized by contacting it with a solution of ethylenediamine or 1,3- diaminopropane in an inert solvent comprising from about 50 to 100 volume percent of a water miscible organic solvent and from 0 to about 50 percent water,
b. contacting the aminated surface with a noble metal salt solution and c.-treating said surface with a reducing agent forming a metallized surface having a resistance of about 100 ohms/sq. or less;
wherein said rubber modified polymer contains about 12 to 40 weight percent rubber, about 12 to 30 weight percent of said acid or anhydride and the balance to make 100 percent of one or more monomers copolymerized therewith and wherein said polymer is the product of polymerizing the monomers in the presence of the rubber in a finely divided form.
2. The process of claim 1 further comprising the step of depositing one or more metallic layers on the metallized surface.
3. The process of claim 1 wherein the noble metal is silver.
4. The process of claim 1 wherein the rubber content is about 16 to 22 percent.
5. The process of claim 1 wherein the acid or anhydride content is about 12 to 25 percent.
6. The process of claim 1 wherein the acid or anhy dride content is about 14 to 20 percent.
7. The process of claim 1 wherein said polymer is a rubber modified polymer of an unsaturated dicarboxylic acid anhydride and a copolymerizable monomer.
8. The process of claim 1 wherein said polymer is a rubber modified styrene-maleic anhydride copolymer.
9. The process of claim 1 wherein said organic solvent is an alcohol.
10. The process of claim 9 wherein said solvent is a 50:50, waterzalcohol mixture.
11. The process of claim wherein said alcohol is methyl alcohol, ethyl alcohol or isopropyl alcohol.
12. A process for metallizing plastic articles formed from a rubber modified unsaturated dicarboxylic acid anhydride containing thermoplastic polymer which comprises the steps of a. aminating the surface to be metallized by contacting it with a solution of ethylenediamine or 1,3- diaminopropane in an inert solvent comprising from about 50 to 100 volume percent of a water miscible organic solvent and from O to about 50 percent water,
b. contacting the aminated surface with a noble metal salt solution and c. treating said surface with a reducing agent forming a metallized surface having a resistance of about ohms/sq. or less;
wherein said rubber modified polymer contains about 12 to 40 weight percent rubber, about 12 to 30 weight percent of said anhydride and the balance to make 100 percent of one or more monomers copolymerizable therewith and wherein said polymer is the product of polymerizing the monomers in the presence of the rubber in a finely divided form.
13. The process of claim 12 further comprising the step of depositing one or more metallic layers on the metallized surface.
14. The process of claim 12 wherein the polymer is a rubber modified polymer of said anhydride and an alkenyl aromatic monomer.
15. The process of claim 14 wherein said polymer is a rubber modified styrene-maleic anhydride polymer.
16. The process of claim 14 wherein said rubber is a styrene-butadiene rubber.
17. The process of claim 14 wherein the rubber comprises about 16 to 22 percent and the anhydride about 14 to 20 percent.
18. The process of claim 12 vent is an alcohol.
19. The process of claim 18 wherein said solvent is a 50:50, waterzalcohol mixture.
20. The process of claim 19 wherein said alcohol is methyl alcohol, ethyl alcohol or isopropyl alcohol.
21. The process of claim 12 wherein the noble metal is silver.
wherein said organic sol-

Claims (21)

1. A PROCESS OR METALLIZING PLASTIC ARTICLES FORMED FROM A RUBBER MODIFIED UNSATURATED CARBOXYLIC ACID OR ANHYDRIDE CONTAINING THERMOPLASTIC POLYMER WHICH COMPRISES THE STEPS OF A. AMINATING THE SURFACE TO BE METALLIZED BY CONTACTING IT WITH A SOLUTION OF ETHYLENEDIAMINE OR 1,3-DIAMINOPROPANE IN AN INERT SOLVENT COMPRISING FROM ABOUT 50 TO 100 VOLUME PERCENT OF A WATER MISCIBLE ORGANIC SOLVENT AND FROM 0 TO ABOUT 50 PERCENT WATER, B. CONTACTING THE AMINATED SURFACE WITH A NOBLE METAL SALT SOLUTION AND C. TREATING SAID SURFACE WITH A REDUCING AGENT FORMNG A METALLIZED SURFACE HAVING A RESISTANCE OF ABOUT 100 OHMS/SQ. OR LESS, WHEREIN SAID RUBBER MODIFIED POLYMER CONTAINS ABOUT 12 TO 40 WEIGHT PERCENT RUBBER, ABOUT 12 TO 30 WEIGHT PRCENT OF SAID ACID OR ANHYDRIDE AND THE BALANCE TO MAKE 100 PERCENT OF ONE OR MORE MONOMERS COPOLYMERIZED THEREWITH AND WHEREIN SAID POLYMER IS THE PRODUCT OF POLYMERIZING THE MONOMENTS IN THE PRESENCE OF THE RUBBER IN A FINELY DIVIDED FORM.
2. The process of claim 1 further comprising the step of depositing one or more metallic layers on the metallized surface.
3. The process of claim 1 wherein the noble metal is silver.
4. The process of claim 1 wherein the rubber content is about 16 to 22 percent.
5. The process of claim 1 wherein the acid or anhydride content is about 12 to 25 percent.
6. The process of claim 1 wherein the acid or anhydride content is about 14 to 20 percent.
7. The process of claim 1 wherein said polymer is a rubber modified polymer of an unsaturated dicarboxylic acid anhydride and a copolymerizable monomer.
8. The process of claim 1 wherein said polymer is a rubber modified styrene-maleic anhydride copolymer.
9. The process of claim 1 wherein said organic solvent is an alcohol.
10. The process of claim 9 wherein said solvent is a 50:50, water:alcohol mixture.
11. The process of claim 10 wherein said alcohol is methyl alcohol, ethyl alcohol or isopropyl alcohol.
12. A process for metallizing plastic articles formed from a rubber modified unsaturated dicarboxylic acid anhydride containing thermoplastic polymer which comprises the steps of a. aminating the surface to be metallized by contacting it with a solution of ethylenediamine or 1,3-diaminopropane in an inert solvent comprising from about 50 to 100 volume percent of a water miscible organic solvent and from 0 to about 50 percent water, b. contacting the aminated surface with a noble metal salt solution and c. treating said surface with a reducing agent forming a metallized surface having a resistance of about 100 ohms/sq. or less; wherein said rubber modified polymer contains about 12 to 40 weight percent rubber, about 12 to 30 weight percent of said anhydride and the balance to make 100 percent of one or more monomers copolymerizable therewith and wherein said polymer is the product of polymerizing the monomers in the presence of the rubber in a finely divided form.
13. The process of claim 12 further comprising the step of depositing one or more metallic layers on the metallized surface.
14. The process of claim 12 wherein the polymer is a rubber modified polymer of said anhydride and an alkenyl aromatic monomer.
15. The process of claim 14 wherein said polymer is a rubber modified styrene-maleic anhydride polymer.
16. The process of claim 14 wherein said rubber is a styrene-butadiene rubber.
17. The process of claim 14 wherein the rubber comprises about 16 to 22 percent and the anhydride about 14 to 20 percent.
18. The process of claim 12 wherein said organic solvent is an alcohol.
19. The process of claim 18 wherein said solvent is a 50:50, water:alcohol mixture.
20. The process of claim 19 wherein said alcohol is methyl alcohol, ethyl alcohol or isopropyl alcohol.
21. The process of claim 12 wherein the noble metal is silver.
US43945374 1974-02-04 1974-02-04 Process of metal plating on plastics Expired - Lifetime US3896252A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US43945374 US3896252A (en) 1974-02-04 1974-02-04 Process of metal plating on plastics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US43945374 US3896252A (en) 1974-02-04 1974-02-04 Process of metal plating on plastics

Publications (1)

Publication Number Publication Date
US3896252A true US3896252A (en) 1975-07-22

Family

ID=23744759

Family Applications (1)

Application Number Title Priority Date Filing Date
US43945374 Expired - Lifetime US3896252A (en) 1974-02-04 1974-02-04 Process of metal plating on plastics

Country Status (1)

Country Link
US (1) US3896252A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4277541A (en) * 1979-10-01 1981-07-07 Monsanto Company Protection of anhydride copolymers
US4312962A (en) * 1981-02-23 1982-01-26 Monsanto Company Adhesion in metal plating
US20050005820A1 (en) * 2003-07-11 2005-01-13 Tom Etheridge Palladium complexes for printing circuits
US6983542B2 (en) 2001-08-24 2006-01-10 Waddington North America, Inc. Metallized cutlery and tableware
US20060191145A1 (en) * 2001-08-24 2006-08-31 Waddington North America, Inc. Metallized cutlery and tableware and method therefor
US20100143732A1 (en) * 2008-12-10 2010-06-10 Xerox Corporation Composite Containing Polymer, Filler and Metal Plating Catalyst, Method of Making Same, and Article Manufactured Therefrom
WO2016103160A1 (en) 2014-12-23 2016-06-30 Sabic Global Technologies B.V. Platable resin compositions

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3222218A (en) * 1962-01-02 1965-12-07 Exxon Research Engineering Co Metal coating process
US3359345A (en) * 1964-11-25 1967-12-19 Rexall Drug Chemical Butadiene-styrene block copolymers reacted with monomeric mixtures
US3567488A (en) * 1969-02-05 1971-03-02 Dow Chemical Co Process for electroless plating of carboxylic acid copolymers using ammonla
US3649713A (en) * 1968-08-23 1972-03-14 Uniroyal Inc Electrolessly plateable polymeric composition
US3702285A (en) * 1968-07-11 1972-11-07 Degussa Process for the pretreatment of plastic for the purpose of adhesive metallization

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3222218A (en) * 1962-01-02 1965-12-07 Exxon Research Engineering Co Metal coating process
US3359345A (en) * 1964-11-25 1967-12-19 Rexall Drug Chemical Butadiene-styrene block copolymers reacted with monomeric mixtures
US3702285A (en) * 1968-07-11 1972-11-07 Degussa Process for the pretreatment of plastic for the purpose of adhesive metallization
US3649713A (en) * 1968-08-23 1972-03-14 Uniroyal Inc Electrolessly plateable polymeric composition
US3567488A (en) * 1969-02-05 1971-03-02 Dow Chemical Co Process for electroless plating of carboxylic acid copolymers using ammonla

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4277541A (en) * 1979-10-01 1981-07-07 Monsanto Company Protection of anhydride copolymers
US4312962A (en) * 1981-02-23 1982-01-26 Monsanto Company Adhesion in metal plating
US8621755B2 (en) 2001-08-24 2014-01-07 Waddington North America, Inc. Metallized cutlery and tableware and method therefor
US6983542B2 (en) 2001-08-24 2006-01-10 Waddington North America, Inc. Metallized cutlery and tableware
US20060191145A1 (en) * 2001-08-24 2006-08-31 Waddington North America, Inc. Metallized cutlery and tableware and method therefor
EP1955620A1 (en) 2001-08-24 2008-08-13 Waddington North America, Inc. Metallized cutlery and tableware
US20100192388A1 (en) * 2001-08-24 2010-08-05 Waddington North America, Inc. Metallized cutlery and tableware and method therefor
US8176641B2 (en) 2001-08-24 2012-05-15 Waddington North America, Inc. Metallized cutlery and tableware and method therefor
US20050005820A1 (en) * 2003-07-11 2005-01-13 Tom Etheridge Palladium complexes for printing circuits
US7537799B2 (en) * 2003-07-11 2009-05-26 Hewlett-Packard Development Company, L.P. Methods of forming electrically conductive pathways using palladium aliphatic amine complexes
US20090249976A1 (en) * 2003-07-11 2009-10-08 Tom Etheridge Palladium complexes for printing circuits
US7896483B2 (en) 2003-07-11 2011-03-01 Hewlett Packard Development Company, L.P. Palladium complexes for printing circuits
US20100143732A1 (en) * 2008-12-10 2010-06-10 Xerox Corporation Composite Containing Polymer, Filler and Metal Plating Catalyst, Method of Making Same, and Article Manufactured Therefrom
US8592043B2 (en) 2008-12-10 2013-11-26 Xerox Corporation Composite containing polymer, filler and metal plating catalyst, method of making same, and article manufactured therefrom
US8383243B2 (en) 2008-12-10 2013-02-26 Xerox Corporation Composite containing polymer, filler and metal plating catalyst, method of making same, and article manufactured therefrom
WO2016103160A1 (en) 2014-12-23 2016-06-30 Sabic Global Technologies B.V. Platable resin compositions

Similar Documents

Publication Publication Date Title
US4148945A (en) Process of metal plating on plastics
US4493861A (en) Process for activating substrate surfaces for currentless metallization
US4764401A (en) Process for activating substrate surfaces for electroless metallization
US4039714A (en) Pretreatment of plastic materials for metal plating
EP2009142B1 (en) Composition for etching treatment of resin molded article
US3998602A (en) Metal plating of polymeric substrates
US3501332A (en) Metal plating of plastics
US3896252A (en) Process of metal plating on plastics
US4832989A (en) Method of improving the bond strength of electrolessly deposited metal layers on plastic-material surfaces
US3505098A (en) Electroplating of polymeric materials having a polymeric primer coating
JPH04259381A (en) Surface reformed synthetic resin material and its production
US3533828A (en) Metal plating of plastic surfaces
US3058845A (en) Process for metallizing polyacrylonitrile shaped article by treating with a water soluble metal salt and reducing the salt to the free metal
TWI404475B (en) Selective deposition of metal on plastic substrates
JPS61210183A (en) Method for providing metal film to surface of polymer
US7645370B2 (en) Plating resin molded article and process for producing the same
KR840000440B1 (en) Plated acrylate styrene acrylonitrile article
US3513015A (en) Prevention of skip plating in an electroless nickel bath
US3562118A (en) Metal plated plastics and process therefor
US3672937A (en) Process for the non-electrolytic metallizing of non-conductors
JPH0247547B2 (en)
US3801478A (en) Process of metallizing polymeric materials
US3741800A (en) Metal plated plastics
US3547785A (en) Treatment of resin surfaces prior to non-electrolytic plating
US3700481A (en) Electrolessly platable polymeric blends